Result

Search results for the GEO ID: GSE17101

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GSM ID

GPL ID

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Title

Source name

Description

Characteristics

GSM426836

GPL1261

non-GIC-1

mouse NSC

strain: C57BL/6 genome/variation: p53-/- developmental stage: E14.5 embryo tissue: brain cell type: neural stem cells nontumorigenic subline: non-Glioma Initiating Cell-like cells

9G_MG430_2_08013001.CEL

Sample_geo_accession	GSM426836
Sample_status	Public on Dec 01 2009
Sample_submission_date	Jul 13 2009
Sample_last_update_date	Oct 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_growth_protocol_ch1	Neuroepithelial cells were prepared from embryonic day 14.5 mouse telencephalon and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM) /F12 medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin, and bFGF as floating spheres. Neural stem cells (NSCs) were transfected with pCMS-EGFP-HRasL61 and pBabe-neo by electroporation and cultured in 0.5 mg/ml neomycin. The GFP-positive stable NSCs (NSCL61s) were purified by flow cytometry.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared using the RNeasy Mini Kit (QIAGEN).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix), according to the manufacturer’s instruction.
Sample_hyb_protocol	Labeled probes were used for the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
Sample_scan_protocol	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
Sample_data_processing	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
Sample_platform_id	GPL1261
Sample_contact_name	Toru,,Kondo
Sample_contact_email	tkondo@cdb.riken.jp
Sample_contact_phone	+81-78-306-3170
Sample_contact_fax	+81-78-306-3171
Sample_contact_laboratory	Laboratory for Cell Lineage Modulation
Sample_contact_department	Center for Developmental Biology
Sample_contact_institute	RIKEN
Sample_contact_address	2-2-3, Minatojima-Minamimachi, Chuo-ku
Sample_contact_city	Kobe
Sample_contact_zip/postal_code	650-0047
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM426nnn/GSM426836/suppl/GSM426836.CEL.gz
Sample_series_id	GSE17062
Sample_series_id	GSE17101
Sample_data_row_count	45101

GSM426837

GPL1261

non-GIC-2

mouse NSC

strain: C57BL/6 genome/variation: p53-/- developmental stage: E14.5 embryo tissue: brain cell type: neural stem cells nontumorigenic subline: non-Glioma Initiating Cell-like cells

10A_MG430_2_08013002.CEL

Sample_geo_accession	GSM426837
Sample_status	Public on Dec 01 2009
Sample_submission_date	Jul 13 2009
Sample_last_update_date	Oct 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_growth_protocol_ch1	Neuroepithelial cells were prepared from embryonic day 14.5 mouse telencephalon and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM) /F12 medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin, and bFGF as floating spheres. Neural stem cells (NSCs) were transfected with pCMS-EGFP-HRasL61 and pBabe-neo by electroporation and cultured in 0.5 mg/ml neomycin. The GFP-positive stable NSCs (NSCL61s) were purified by flow cytometry.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared using the RNeasy Mini Kit (QIAGEN).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix), according to the manufacturer’s instruction.
Sample_hyb_protocol	Labeled probes were used for the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
Sample_scan_protocol	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
Sample_data_processing	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
Sample_platform_id	GPL1261
Sample_contact_name	Toru,,Kondo
Sample_contact_email	tkondo@cdb.riken.jp
Sample_contact_phone	+81-78-306-3170
Sample_contact_fax	+81-78-306-3171
Sample_contact_laboratory	Laboratory for Cell Lineage Modulation
Sample_contact_department	Center for Developmental Biology
Sample_contact_institute	RIKEN
Sample_contact_address	2-2-3, Minatojima-Minamimachi, Chuo-ku
Sample_contact_city	Kobe
Sample_contact_zip/postal_code	650-0047
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM426nnn/GSM426837/suppl/GSM426837.CEL.gz
Sample_series_id	GSE17062
Sample_series_id	GSE17101
Sample_data_row_count	45101

GSM426838

GPL1261

GIC-1

mouse NSC

strain: C57BL/6 genome/variation: p53-/- developmental stage: E14.5 embryo tissue: brain cell type: neural stem cells tumorigenic subline: Glioma Initiating Cell-like cells

6B_MG430_2_08013003.CEL

Sample_geo_accession	GSM426838
Sample_status	Public on Dec 01 2009
Sample_submission_date	Jul 13 2009
Sample_last_update_date	Oct 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_growth_protocol_ch1	Neuroepithelial cells were prepared from embryonic day 14.5 mouse telencephalon and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM) /F12 medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin, and bFGF as floating spheres. Neural stem cells (NSCs) were transfected with pCMS-EGFP-HRasL61 and pBabe-neo by electroporation and cultured in 0.5 mg/ml neomycin. The GFP-positive stable NSCs (NSCL61s) were purified by flow cytometry.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared using the RNeasy Mini Kit (QIAGEN).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix), according to the manufacturer’s instruction.
Sample_hyb_protocol	Labeled probes were used for the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
Sample_scan_protocol	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
Sample_data_processing	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
Sample_platform_id	GPL1261
Sample_contact_name	Toru,,Kondo
Sample_contact_email	tkondo@cdb.riken.jp
Sample_contact_phone	+81-78-306-3170
Sample_contact_fax	+81-78-306-3171
Sample_contact_laboratory	Laboratory for Cell Lineage Modulation
Sample_contact_department	Center for Developmental Biology
Sample_contact_institute	RIKEN
Sample_contact_address	2-2-3, Minatojima-Minamimachi, Chuo-ku
Sample_contact_city	Kobe
Sample_contact_zip/postal_code	650-0047
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM426nnn/GSM426838/suppl/GSM426838.CEL.gz
Sample_series_id	GSE17062
Sample_series_id	GSE17101
Sample_data_row_count	45101

GSM426839

GPL1261

GIC-2

mouse NSC

strain: C57BL/6 genome/variation: p53-/- developmental stage: E14.5 embryo tissue: brain cell type: neural stem cells tumorigenic subline: Glioma Initiating Cell-like cells

8B_MG430_2_08013004.CEL

Sample_geo_accession	GSM426839
Sample_status	Public on Dec 01 2009
Sample_submission_date	Jul 13 2009
Sample_last_update_date	Oct 22 2010
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_growth_protocol_ch1	Neuroepithelial cells were prepared from embryonic day 14.5 mouse telencephalon and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM) /F12 medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin, and bFGF as floating spheres. Neural stem cells (NSCs) were transfected with pCMS-EGFP-HRasL61 and pBabe-neo by electroporation and cultured in 0.5 mg/ml neomycin. The GFP-positive stable NSCs (NSCL61s) were purified by flow cytometry.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared using the RNeasy Mini Kit (QIAGEN).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix), according to the manufacturer’s instruction.
Sample_hyb_protocol	Labeled probes were used for the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
Sample_scan_protocol	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
Sample_data_processing	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
Sample_platform_id	GPL1261
Sample_contact_name	Toru,,Kondo
Sample_contact_email	tkondo@cdb.riken.jp
Sample_contact_phone	+81-78-306-3170
Sample_contact_fax	+81-78-306-3171
Sample_contact_laboratory	Laboratory for Cell Lineage Modulation
Sample_contact_department	Center for Developmental Biology
Sample_contact_institute	RIKEN
Sample_contact_address	2-2-3, Minatojima-Minamimachi, Chuo-ku
Sample_contact_city	Kobe
Sample_contact_zip/postal_code	650-0047
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM426nnn/GSM426839/suppl/GSM426839.CEL.gz
Sample_series_id	GSE17062
Sample_series_id	GSE17101
Sample_data_row_count	45101

GSM427234

GPL1261

NSCL61-1

mouse NSC

strain: C57BL/6 genome/variation: p53-/- developmental stage: E14.5 embryo tissue: brain cell type: Neural Stem Cells, Glioma Initiating Cell-like cell line: NSCL61

NSC-L61-cont-1_M430_2_08080101.CEL

Sample_geo_accession	GSM427234
Sample_status	Public on Dec 01 2009
Sample_submission_date	Jul 14 2009
Sample_last_update_date	Jul 14 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_growth_protocol_ch1	Neuroepithelial cells were prepared from embryonic day 14.5 mouse telencephalon and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM)/F12 medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin, and bFGF as floating spheres.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared using the RNeasy Mini Kit (QIAGEN).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix) according to the manufacturer’s instruction.
Sample_hyb_protocol	Labeled probes were hybridized to the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
Sample_scan_protocol	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
Sample_data_processing	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
Sample_platform_id	GPL1261
Sample_contact_name	Toru,,Kondo
Sample_contact_email	tkondo@cdb.riken.jp
Sample_contact_phone	+81-78-306-3170
Sample_contact_fax	+81-78-306-3171
Sample_contact_laboratory	Laboratory for Cell Lineage Modulation
Sample_contact_department	Center for Developmental Biology
Sample_contact_institute	RIKEN
Sample_contact_address	2-2-3, Minatojima-Minamimachi, Chuo-ku
Sample_contact_city	Kobe
Sample_contact_zip/postal_code	650-0047
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM427nnn/GSM427234/suppl/GSM427234.CEL.gz
Sample_series_id	GSE17076
Sample_series_id	GSE17101
Sample_data_row_count	45101

GSM427235

GPL1261

NSCL61-2

mouse NSC

strain: C57BL/6 genome/variation: p53-/- developmental stage: E14.5 embryo tissue: brain cell type: Neural Stem Cells, Glioma Initiating Cell-like cell line: NSCL61

NSC-L61-cont-2_M430_2_08080102.CEL

Sample_geo_accession	GSM427235
Sample_status	Public on Dec 01 2009
Sample_submission_date	Jul 14 2009
Sample_last_update_date	Jul 14 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_growth_protocol_ch1	Neuroepithelial cells were prepared from embryonic day 14.5 mouse telencephalon and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM)/F12 medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin, and bFGF as floating spheres.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared using the RNeasy Mini Kit (QIAGEN).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix) according to the manufacturer’s instruction.
Sample_hyb_protocol	Labeled probes were hybridized to the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
Sample_scan_protocol	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
Sample_data_processing	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
Sample_platform_id	GPL1261
Sample_contact_name	Toru,,Kondo
Sample_contact_email	tkondo@cdb.riken.jp
Sample_contact_phone	+81-78-306-3170
Sample_contact_fax	+81-78-306-3171
Sample_contact_laboratory	Laboratory for Cell Lineage Modulation
Sample_contact_department	Center for Developmental Biology
Sample_contact_institute	RIKEN
Sample_contact_address	2-2-3, Minatojima-Minamimachi, Chuo-ku
Sample_contact_city	Kobe
Sample_contact_zip/postal_code	650-0047
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM427nnn/GSM427235/suppl/GSM427235.CEL.gz
Sample_series_id	GSE17076
Sample_series_id	GSE17101
Sample_data_row_count	45101

GSM427236

GPL1261

NSCL61-sox11-1

mouse NSC

strain: C57BL/6 genome/variation: p53-/-, sox11-expressing developmental stage: E14.5 embryo tissue: brain cell type: Neural Stem Cells, Glioma Initiating Cell-like cell line: NSCL61-sox11

NSC-L61-s11-314-1_M430_2_08080103.CEL

Sample_geo_accession	GSM427236
Sample_status	Public on Dec 01 2009
Sample_submission_date	Jul 14 2009
Sample_last_update_date	Jul 14 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_growth_protocol_ch1	Neuroepithelial cells were prepared from embryonic day 14.5 mouse telencephalon and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM)/F12 medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin, and bFGF as floating spheres.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared using the RNeasy Mini Kit (QIAGEN).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix) according to the manufacturer’s instruction.
Sample_hyb_protocol	Labeled probes were hybridized to the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
Sample_scan_protocol	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
Sample_data_processing	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
Sample_platform_id	GPL1261
Sample_contact_name	Toru,,Kondo
Sample_contact_email	tkondo@cdb.riken.jp
Sample_contact_phone	+81-78-306-3170
Sample_contact_fax	+81-78-306-3171
Sample_contact_laboratory	Laboratory for Cell Lineage Modulation
Sample_contact_department	Center for Developmental Biology
Sample_contact_institute	RIKEN
Sample_contact_address	2-2-3, Minatojima-Minamimachi, Chuo-ku
Sample_contact_city	Kobe
Sample_contact_zip/postal_code	650-0047
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM427nnn/GSM427236/suppl/GSM427236.CEL.gz
Sample_series_id	GSE17076
Sample_series_id	GSE17101
Sample_data_row_count	45101

GSM427237

GPL1261

NSCL61-sox11-2

mouse NSC

strain: C57BL/6 genome/variation: p53-/-, sox11-expressing developmental stage: E14.5 embryo tissue: brain cell type: Neural Stem Cells, Glioma Initiating Cell-like cell line: NSCL61-sox11

NSC-L61-s11-314-2_M430_2_08080104.CEL

Sample_geo_accession	GSM427237
Sample_status	Public on Dec 01 2009
Sample_submission_date	Jul 14 2009
Sample_last_update_date	Jul 14 2009
Sample_type	RNA
Sample_channel_count	1
Sample_organism_ch1	Mus musculus
Sample_taxid_ch1	10090
Sample_growth_protocol_ch1	Neuroepithelial cells were prepared from embryonic day 14.5 mouse telencephalon and expanded in serum-free Dulbecco's Modified Eagle's medium (DMEM)/F12 medium containing bovine insulin (10 μg/ml), human transferrin (100 μg/ml), BSA (100 μg/ml), progesterone (60 ng/ml), putrescine (16 μg/ml), sodium selenite (40 ng/ml), N-acetylcysteine (60 μg/ml), forskolin (5 μM), PDGF (10 ng/ml), penicillin, streptomycin, and bFGF as floating spheres.
Sample_molecule_ch1	total RNA
Sample_extract_protocol_ch1	Total RNA was prepared using the RNeasy Mini Kit (QIAGEN).
Sample_label_ch1	biotin
Sample_label_protocol_ch1	Five micrograms of total RNA were labeled with biotin by in vitro transcription (IVT) using the One-Cycle Target Labeling procedure for biotin labeling by in vitro transcription (Affymetrix) according to the manufacturer’s instruction.
Sample_hyb_protocol	Labeled probes were hybridized to the GeneChip Mouse Genome 430 2.0 array (Affymetrix) according to the manufacturer’s instructions.
Sample_scan_protocol	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data.
Sample_data_processing	The microarray image data were processed with the GeneChip Scanner 3000 (Affymetrix) to generate CEL data. The CEL data were then analyzed with dChip software, which can normalize and process multiple datasets simultaneously.
Sample_platform_id	GPL1261
Sample_contact_name	Toru,,Kondo
Sample_contact_email	tkondo@cdb.riken.jp
Sample_contact_phone	+81-78-306-3170
Sample_contact_fax	+81-78-306-3171
Sample_contact_laboratory	Laboratory for Cell Lineage Modulation
Sample_contact_department	Center for Developmental Biology
Sample_contact_institute	RIKEN
Sample_contact_address	2-2-3, Minatojima-Minamimachi, Chuo-ku
Sample_contact_city	Kobe
Sample_contact_zip/postal_code	650-0047
Sample_contact_country	Japan
Sample_supplementary_file	ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM427nnn/GSM427237/suppl/GSM427237.CEL.gz
Sample_series_id	GSE17076
Sample_series_id	GSE17101
Sample_data_row_count	45101

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